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Design and Synthesis of Small Molecules as Potent Staphylococcus aureus Sortase A Inhibitors
被引:27
|作者:
Ha, Min Woo
[1
,2
]
Yi, Sung Wook
[3
]
Paek, Seung-Mann
[4
,5
]
机构:
[1] Jeju Natl Univ, Coll Pharm, 102 Jejudaehak Ro, Jeju 63243, Jeju Do, South Korea
[2] Jeju Natl Univ, Interdisciplinary Grad Program Adv Convergence Te, 102 Jejudaehak Ro, Jeju 63243, Jeju Do, South Korea
[3] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[4] Gyeongsang Natl Univ, Coll Pharm, Jinju Daero 501, Jinju 52828, Gyeongsangnam D, South Korea
[5] Gyeongsang Natl Univ, Res Inst Pharmaceut Sci, Jinju Daero 501, Jinju 52828, Gyeongsangnam D, South Korea
来源:
ANTIBIOTICS-BASEL
|
2020年
/
9卷
/
10期
基金:
新加坡国家研究基金会;
关键词:
drug resistant;
sortase A;
Staphylococcus aureus;
sortase A inhibitor;
small organic molecule;
synthetic chemistry;
SORTING SIGNAL BINDING;
SURFACE-PROTEINS;
CELL-WALL;
ANTIBIOTIC-RESISTANCE;
BIOLOGICAL EVALUATION;
TRANSPEPTIDASE SRTA;
DRUG DISCOVERY;
MANNICH-BASES;
MECHANISM;
DERIVATIVES;
D O I:
10.3390/antibiotics9100706
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
The widespread and uncontrollable emergence of antibiotic-resistant bacteria, especially methicillin-resistant Staphylococcus aureus, has promoted a wave of efforts to discover a new generation of antibiotics that prevent or treat bacterial infections neither as bactericides nor bacteriostats. Due to its crucial role in virulence and its nonessentiality in bacterial survival, sortase A has been considered as a great target for new antibiotics. Sortase A inhibitors have emerged as promising alternative antivirulence agents against bacteria. Herein, the structural and preparative aspects of some small synthetic organic compounds that block the pathogenic action of sortase A have been described.
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页码:1 / 16
页数:16
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